A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698698



Internal ID15088664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53419262..53510924hg38UCSC Ensembl
Innerchr19:53922515..54014178hg19UCSC Ensembl
Innerchr19:58614327..58705990hg18UCSC Ensembl
Innerchr19:58614327..58705990hg17UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3891663
hg1991664
hg1891664
hg1791664
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515728
Supporting Variants
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698698
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer